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Hydroxyapatite porous scaffold engineered with biological polymer hybrid coating for antibiotic Vancomycin release

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Abstract

The purpose of this study is to improve hydroxyapatite (HA) porous scaffolds via coating with biological polymer-HA hybrids for use as wound healing and tissue regeneration. Highly porous HA scaffolds, fabricated by a polyurethane foam reticulate method, were coated with hybrid coating solution, consisting of poly(ε-caprolactone) (PCL), HA powders, and the antibiotic Vancomycin. The PCL to HA ratio was fixed at 1.5 and the drug amounts were varied [drug/(PCL + HA) = 0.02 and 0.04]. For the purpose of comparison, bare HA scaffold without the hybrid coating layer was also loaded with Vancomycin via an immersion-adsorption method. The hybrid coating structure and morphology were observed with Fourier transformed infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM). The effects of the hybrid coating on the compressive mechanical properties and the in vitro drug release of the scaffolds were investigated in comparison with bare HA scaffold. The PCL-HA hybrid coating altered the scaffold pore structure slightly, resulting in thicker stems and reduced porosity. With the hybrid coating, the HA scaffold responded to an applied compressive stress more effectively without showing a brittle failure. This was attributed to the shielding and covering of the framework surface by the coating layer. The encapsulated drugs within the coated scaffold was released in a highly sustained manner as compared to the rapid release of drugs directly adsorbed on the pure HA scaffold. These findings suggest that the coated HA scaffolds expand their applicability in hard tissue regeneration and wound healing substitutes delivering bioactive molecules.

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References

  1. R. LANGER and J. P. VACANTI, Science 260 (1993) 920.

    CAS  PubMed  Google Scholar 

  2. Y. KIMURA, Biodegradable polymers, in “Biomedical Applications in Polymeric Materials,” edited by T. Tsuruta (CRC Press, Boca Raton, 1993) p. 163.

    Google Scholar 

  3. L. L. HENCH, J. Amer. Ceram. Soc. 74 (1991) 1487.

    Google Scholar 

  4. H.-W. KIM, Y.-J. NOH, Y.-H. KOH and H.-E. KIM, J. Mater. Sci.: Mater. Med. 14 (2003) 899.

    Google Scholar 

  5. H.-W. KIM, S.-Y. LEE, C.-J. BAE, Y.-J. NOH, H.-E. KIM, H.-M. KIM and J. KO, Biomater. 24 (2003) 3277.

    Google Scholar 

  6. J. C. KNOWLES, J. Mater. Chem. 10 (2003) 2395.

    Google Scholar 

  7. M. S. PARK, E. D. EANES, J. M. ANTONUCCU and D. SKRTIC, Dent. Mater. 14 (1998) 137.

    Google Scholar 

  8. C. DOMINGO, R. W. ARCIS, E. OSORIO et al., Dent. Mater. 19 (2003) 478.

    Google Scholar 

  9. Y. TABATA, Necessity of drug delivery systems to tissue engineering, in “Biomaterials and Drug Delivery Toward the New Millennium,” edited by K. D. Park (Han Rim Won Publisher, Seoul, Korea, 2000) p. 531.

    Google Scholar 

  10. G. GREENSTEIN and A. POLSON, J. Period. 69 (1998) 507.

    Google Scholar 

  11. A. BARROUG and M. J. GLIMCHER, J. Orthopaed. Res. 20 (2002) 274.

    Google Scholar 

  12. V. S. KOMLEV, S. M. BARINOV and E. V. KOPLIK, Biomater. 23 (2002) 3449.

    Google Scholar 

  13. A. C. QUEIROZ, J. D. SANTOS, F. J. MONTEIRO, I. R. GIBSON and J. C. KNOWLES, Biomater. 22 (2001) 1393.

    Google Scholar 

  14. C. G. PITT, Poly(ε-caprolactone) and its copolymers. in “Biodegradable Polymers as Drug Delivery Systems,” edited by M. Chasin and R. Lange (Marcel Dekker, New York, 1990) p. 71.

    Google Scholar 

  15. G. L. COOPER and D. B. Given, Vancomycin, “A Comprehensive Review of 30 Years of Clinical Experience” (Eli Lilly, 1986) p. 39.

  16. H.-W. KIM, J. C. KNOWLES and H.-E. KIM, Biomater. 25 (2004) 1279.

    Google Scholar 

  17. P. KENESEI, CS. KADAR, ZS. RAJKOVITS and J. LENDVAI, Script. Mater. 50 (2004) 295.

    Google Scholar 

  18. M. THOMAS, IN “ULTRAVIOLET and VISIBLE SPECTROSCOPY,” 2ND ED., EDITED BY D. J. ANDO (WILEY, ENGLAND, 1996) P. 16.

    Google Scholar 

  19. L. MONTANARO, Y. JORAND, G. FANTOZZI and A. NEGRO, J. Eur. Ceram. Soc. 18 (1998) 1339.

    Google Scholar 

  20. T. J. LIM, B. SMITH and D. L. MCDOWELL, Acta. Mater. 50 (2002) 2867.

    Google Scholar 

  21. H.-W. KIM, Y. DENG, P. MIRANDA, A. PAJARES, D. K. KIM, H.-E. KIM and B. R. LAWM, J. Amer. Ceram. Soc. 84 (2001) 2377.

    Google Scholar 

  22. D. H. ROACH, S. LATHABAI and B. R. LAWN, J. Amer. Ceram. Soc. 71 (1988) 97.

    Google Scholar 

  23. P. TADDEI, R. SIMONI and G. FINI, J. Mol. Struct. 565 (2001) 317.

    Google Scholar 

  24. N. PEPPAS and R. L. RITGER, J. Control. Rel. 5 (1987) 37.

    Google Scholar 

  25. F. G. HUTCHINSON and B. J. A. FUR, J. Control. Rel. 13 (1990) 279.

    Google Scholar 

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Correspondence to Hae-Won Kim.

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Kim, HW., Knowles, J.C. & Kim, HE. Hydroxyapatite porous scaffold engineered with biological polymer hybrid coating for antibiotic Vancomycin release. J Mater Sci: Mater Med 16, 189–195 (2005). https://doi.org/10.1007/s10856-005-6679-y

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  • DOI: https://doi.org/10.1007/s10856-005-6679-y

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